Variant report

Variant	esv2761961
Chromosome Location	chr17:46742149-46763403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:46749100-46749225	HepG2	liver:	n/a	n/a
2	ATF2	chr17:46749092-46749366	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:46755667-46756098	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr17:46749085-46749377	GM12878	blood:	n/a	chr17:46749158-46749167
5	BHLHE40	chr17:46755814-46756094	K562	blood:	n/a	chr17:46755955-46755971
6	BRCA1	chr17:46755860-46756069	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr17:46756009-46756032	HepG2	liver:	n/a	n/a
8	CCNT2	chr17:46755799-46756128	K562	blood:	n/a	chr17:46756112-46756121
9	CEBPB	chr17:46754477-46754981	A549	lung:	n/a	chr17:46754919-46754932
10	CEBPB	chr17:46754582-46754855	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr17:46755847-46756217	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr17:46754550-46754874	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr17:46754495-46754902	MCF-7	breast:	n/a	n/a
14	CEBPB	chr17:46754523-46754901	A549	lung:	n/a	n/a
15	CEBPB	chr17:46754540-46754875	IMR90	lung:	n/a	n/a
16	CEBPB	chr17:46754583-46754848	HepG2	liver:	n/a	n/a
17	CEBPB	chr17:46754615-46754895	K562	blood:	n/a	n/a
18	CHD2	chr17:46755909-46756145	HepG2	liver:	n/a	n/a
19	CREB1	chr17:46755800-46756175	A549	lung:	n/a	n/a
20	CREB1	chr17:46749093-46749281	A549	lung:	n/a	n/a
21	CTCF	chr17:46749100-46749250	HepG2	liver:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
22	CTCF	chr17:46756220-46756370	GM12866	blood:	n/a	n/a
23	CTCF	chr17:46749060-46749210	Caco-2	colon:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
24	CTCF	chr17:46755900-46756050	GM06990	blood:	n/a	chr17:46755959-46755977
25	CTCF	chr17:46755592-46755738	GM19240	blood:	n/a	n/a
26	CTCF	chr17:46755747-46756114	GM19240	blood:	n/a	chr17:46755959-46755977
27	CTCF	chr17:46755824-46756093	Hela-S3	cervix:	n/a	chr17:46755959-46755977
28	CTCF	chr17:46755920-46756070	HRPEpiC	eye:	n/a	chr17:46755959-46755977
29	CTCF	chr17:46749080-46749230	GM12867	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
30	CTCF	chr17:46749030-46749282	LNCaP	prostate:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
31	CTCF	chr17:46749060-46749210	HFF	foreskin:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
32	CTCF	chr17:46748988-46749374	A549	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
33	CTCF	chr17:46746740-46746890	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr17:46755837-46756089	LNCaP	prostate:	n/a	chr17:46755959-46755977
35	CTCF	chr17:46749032-46749309	Kidney_OC	kidney:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
36	CTCF	chr17:46755420-46755570	GM12864	blood:	n/a	chr17:46755421-46755434
37	CTCF	chr17:46749100-46749250	HCPEpiC	choroid plexus:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
38	CTCF	chr17:46755940-46756090	HCFaa	heart:	n/a	chr17:46755959-46755977
39	CTCF	chr17:46749063-46749294	GM19239	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
40	CTCF	chr17:46755900-46756050	GM12868	blood:	n/a	chr17:46755959-46755977
41	CTCF	chr17:46755240-46755390	AG09319	gingival:	n/a	n/a
42	CTCF	chr17:46755880-46756030	AoAF	blood vessel:	n/a	chr17:46755959-46755977
43	CTCF	chr17:46749060-46749210	HEK293	kidney:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
44	CTCF	chr17:46749031-46749316	Pancreas_OC	pancreas:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
45	CTCF	chr17:46755738-46756183	K562	blood:	n/a	chr17:46755959-46755977
46	CTCF	chr17:46755736-46756118	Gliobla	brain:	n/a	chr17:46755959-46755977
47	CTCF	chr17:46755900-46756050	GM12874	blood:	n/a	chr17:46755959-46755977
48	CTCF	chr17:46755880-46756030	GM12801	blood:	n/a	chr17:46755959-46755977
49	CTCF	chr17:46749020-46749327	MCF-7	breast:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
50	CTCF	chr17:46749049-46749301	GM20000	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46755719-46755769	BJ	skin:	n/a
2	chr17:46758520-46758570	SKMC	muscle:	n/a
3	chr17:46755566-46755616	AoSMC	blood vessel:	n/a
4	chr17:46755566-46755616	NT2-D1	testis:	n/a
5	chr17:46755422-46755472	Jurkat	blood:	n/a
6	chr17:46756094-46756144	NT2-D1	testis:	n/a
7	chr17:46753282-46753332	MCF10A-Er-Src	breast:	n/a
8	chr17:46756001-46756051	NHBE	bronchial:	n/a
9	chr17:46756001-46756051	PANC-1	pancreas:	n/a
10	chr17:46756094-46756144	A549	lung:	n/a
11	chr17:46755719-46755769	HRCEpiC	kidney:	n/a
12	chr17:46755719-46755769	HCT-116	colon:	n/a
13	chr17:46755786-46755836	Hepatocyte	liver:	n/a
14	chr17:46756001-46756051	HCM	heart:	n/a
15	chr17:46755422-46755472	GM06990	blood:	n/a
16	chr17:46755422-46755472	ovcar-3	ovarian:	n/a
17	chr17:46753282-46753332	GM06990	blood:	n/a
18	chr17:46755566-46755616	GM12878	blood:	n/a
19	chr17:46758520-46758570	IMR90	lung:	fetal
20	chr17:46756001-46756051	HL-60	blood:	n/a
21	chr17:46756001-46756051	RPTEC	kidney:	n/a
22	chr17:46755422-46755472	SAEC	small airway:	n/a
23	chr17:46755719-46755769	Hela-S3	cervix:	n/a
24	chr17:46755719-46755769	T-47D	breast:	n/a
25	chr17:46758520-46758570	GM06990	blood:	n/a
26	chr17:46755719-46755769	AG10803	skin:	n/a
27	chr17:46755422-46755472	AoSMC	blood vessel:	n/a
28	chr17:46755786-46755836	CMK	blood:	n/a
29	chr17:46755566-46755616	HCPEpiC	choroid plexus:	n/a
30	chr17:46755566-46755616	HNPCEpiC	eye:	n/a
31	chr17:46755422-46755472	AG09309	skin:	n/a
32	chr17:46758520-46758570	HCF	heart:	n/a
33	chr17:46755566-46755616	HEK293	kidney:	embryo
34	chr17:46755566-46755616	PrEC	prostate:	n/a
35	chr17:46756001-46756051	HPAEpiC	pulmonary alveolar:	n/a
36	chr17:46755719-46755769	PANC-1	pancreas:	n/a
37	chr17:46755422-46755472	HPAEpiC	pulmonary alveolar:	n/a
38	chr17:46756094-46756144	SAEC	small airway:	n/a
39	chr17:46755786-46755836	HepG2	liver:	n/a
40	chr17:46753282-46753332	AG04449	skin:	fetal
41	chr17:46755786-46755836	H1-hESC	embryonic stem cell:	embryo
42	chr17:46756001-46756051	PrEC	prostate:	n/a
43	chr17:46755566-46755616	PFSK-1	brain:	n/a
44	chr17:46755719-46755769	RPTEC	kidney:	n/a
45	chr17:46755719-46755769	SAEC	small airway:	n/a
46	chr17:46753282-46753332	BE2_C	brain:	n/a
47	chr17:46758520-46758570	GM12878	blood:	n/a
48	chr17:46755566-46755616	U87	brain:	n/a
49	chr17:46756001-46756051	Hela-S3	cervix:	n/a
50	chr17:46755422-46755472	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:46749857..46752584-chr17:46924851..46927771,2	K562	blood:
2	chr17:46748727..46749627-chr17:46867991..46868777,6	MCF-7	breast:
3	chr17:46706915..46708436-chr17:46753619..46755678,2	K562	blood:
4	chr17:46748711..46749583-chr17:46956106..46956875,4	MCF-7	breast:
5	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
6	chr17:46755465..46756849-chr17:46867926..46869081,19	MCF-7	breast:
7	chr17:46713679..46714197-chr17:46749118..46749636,2	MCF-7	breast:
8	chr17:46755541..46756386-chr17:46881997..46882806,2	MCF-7	breast:
9	chr17:46748726..46749588-chr17:46801756..46802493,2	K562	blood:
10	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
11	chr17:46702462..46704437-chr17:46745558..46748045,2	K562	blood:
12	chr17:46754810..46756534-chr17:46956012..46957174,7	MCF-7	breast:
13	chr17:46679617..46680600-chr17:46748738..46749566,2	K562	blood:
14	chr17:46755112..46756375-chr17:46868085..46869415,8	MCF-7	breast:
15	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
16	chr17:46693389..46695056-chr17:46744998..46747380,2	K562	blood:
17	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
18	chr17:46755434..46756698-chr17:46954846..46957173,15	K562	blood:
19	chr17:46753552..46755878-chr17:46875165..46876959,2	K562	blood:
20	chr17:46749070..46750038-chr17:46868565..46869067,2	MCF-7	breast:
21	chr17:46755482..46756508-chr17:46867920..46869021,7	K562	blood:
22	chr17:46748703..46749676-chr17:46867980..46869288,6	K562	blood:
23	chr17:46755465..46756352-chr17:46801247..46802560,4	MCF-7	breast:
24	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALCOCO2-4	chr17:46760729-46760779	ENSG00000262745.1

Variant related genes	Relation type
ENSG00000262745	TF binding region
ENSG00000262745	CpG island
ENSG00000170689	chromatin interactions
ENSG00000136436	chromatin interactions
ENSG00000263602	chromatin interactions
ENSG00000233101	chromatin interactions

Extended variants
information (count: 752 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:752 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567708623	chr17:46742152-46742153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529114935	chr17:46742188-46742189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549155860	chr17:46742215-46742216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138381978	chr17:46742250-46742251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111280647	chr17:46742251-46742252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532256298	chr17:46742263-46742264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs397703193	chr17:46742283-46742284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139904894	chr17:46742284-46742285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537731078	chr17:46742321-46742322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4793966	chr17:46742357-46742358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs376705104	chr17:46742382-46742383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4793967	chr17:46742394-46742395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs111527411	chr17:46742516-46742517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112451223	chr17:46742518-46742519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115556435	chr17:46742522-46742523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374523949	chr17:46742566-46742567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4793968	chr17:46742568-46742569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547469573	chr17:46742572-46742573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140189048	chr17:46742578-46742579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542881809	chr17:46742579-46742580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556781480	chr17:46742591-46742592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576678179	chr17:46742601-46742602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189002369	chr17:46742602-46742603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565534064	chr17:46742650-46742651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560369437	chr17:46742669-46742670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527692892	chr17:46742679-46742680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541403178	chr17:46742699-46742700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561269674	chr17:46742757-46742758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530186023	chr17:46742769-46742770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59401592	chr17:46742809-46742810	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs373593149	chr17:46742818-46742819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149885152	chr17:46742828-46742829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566973960	chr17:46742861-46742862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368076921	chr17:46742955-46742956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575566926	chr17:46742963-46742964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371601088	chr17:46742995-46742996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374879107	chr17:46743010-46743011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149010684	chr17:46743013-46743014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376565141	chr17:46743037-46743038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553708571	chr17:46743052-46743053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147106414	chr17:46743079-46743080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536364024	chr17:46743142-46743143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191976886	chr17:46743164-46743165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71369204	chr17:46743213-46743214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs386797494	chr17:46743214-46743215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149869859	chr17:46743215-46743216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78727174	chr17:46743216-46743217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372661730	chr17:46743217-46743218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373025758	chr17:46743223-46743224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576715317	chr17:46743247-46743248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46725600-46749000	Weak transcription	A549	lung
2	chr17:46732600-46748800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr17:46743800-46744600	Bivalent Enhancer	HepG2	liver
4	chr17:46744200-46744400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
5	chr17:46744200-46744400	Bivalent Enhancer	Stomach Mucosa	stomach
6	chr17:46746400-46746600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
7	chr17:46748000-46748200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr17:46748200-46749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr17:46748800-46749000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr17:46748800-46749200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
11	chr17:46748800-46749200	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr17:46748800-46749200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
13	chr17:46748800-46749600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr17:46749000-46749200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:46749000-46749200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:46749000-46749200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr17:46749000-46749200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
18	chr17:46749000-46749200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr17:46749000-46749200	Enhancers	Liver	Liver
20	chr17:46749000-46749200	Enhancers	Brain Germinal Matrix	brain
21	chr17:46749000-46749200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr17:46749000-46749200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
23	chr17:46749000-46749200	Active TSS	HSMM	muscle
24	chr17:46749000-46749400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
25	chr17:46749000-46749400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr17:46749000-46749400	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr17:46749000-46749400	Active TSS	A549	lung
28	chr17:46749000-46749400	Active TSS	HSMMtube	muscle
29	chr17:46749000-46749600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
30	chr17:46749000-46749600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr17:46749000-46749600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr17:46749000-46749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:46749000-46749600	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr17:46749000-46749800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr17:46749000-46749800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr17:46749200-46749400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
37	chr17:46749200-46749400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:46749200-46749400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr17:46749200-46749400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr17:46749200-46749400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
41	chr17:46749200-46749400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
42	chr17:46749200-46749400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:46749200-46749400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr17:46749200-46749400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
45	chr17:46749200-46749400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
46	chr17:46749200-46749400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr17:46749200-46749400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
48	chr17:46749200-46749400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
49	chr17:46749200-46749400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr17:46749200-46749400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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